Laerdal Suction Unit

FDA 510(k) K840110 · Laerdal Medical Corp.

Substantially Equivalent

510(k) numberK840110

Submission

Device name
Laerdal Suction Unit
Applicant
Laerdal Medical Corp.
Mchenry, IL, US
Received
January 10, 1984
Decision date
March 12, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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Questions and answers

When was Laerdal Suction Unit cleared by the FDA?

Laerdal Suction Unit (K840110) received a 510(k) decision of Substantially Equivalent on March 12, 1984, 62 days after the submission was received.

What is the product code of K840110?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.